Canonical Allele Identifier: CA2677955016
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355149del , CM000668.2:g.31355149del GRCh38
NC_000006.11:g.31322926del , CM000668.1:g.31322926del GRCh37
NC_000006.10:g.31430905del NCBI36
NG_023187.1:g.7065del

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.3018del
ENST00000481849.6:n.2537del
ENST00000497377.6:n.2444del
ENST00000640094.2:c.895+169del ENSP00000491275.2:n.895+169del
ENST00000696558.1:c.1040del ENSP00000512716.1:n.1040del
ENST00000696559.1:c.971del ENSP00000512717.1:p.Gly324GlufsTer7
ENST00000696560.1:c.971del ENSP00000512718.1:p.Gly324GlufsTer7
ENST00000696561.1:c.971del ENSP00000512719.1:p.Gly324GlufsTer7
ENST00000696562.1:c.971del ENSP00000512720.1:p.Gly324GlufsTer7
ENST00000412585.7:c.971del MANE Select ENSP00000399168.2:p.Gly324GlufsTer7
ENST00000640094.1:c.88+169del ENSP00000491275.1:n.88+169del
ENST00000412585.6:c.971del ENSP00000399168.2:p.Gly324GlufsTer7
ENST00000463574.1:n.562del
NM_005514.6:c.971del NP_005505.2:p.Gly324GlufsTer7
XM_011514556.1:c.1004del XP_011512858.1:p.Gly335GlufsTer7
XM_011514557.1:c.895+169del XP_011512859.1:n.895+169del
XR_926175.1:n.1410del
NM_005514.7:c.971del NP_005505.2:p.Gly324GlufsTer7
NM_005514.8:c.971del MANE Select NP_005505.2:p.Gly324GlufsTer7